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升主动脉瘤组织中微小RNA表达的无偏倚概况确定了导致该病理过程的分子途径。

Unbiased Profile of MicroRNA Expression in Ascending Aortic Aneurysm Tissue Appoints Molecular Pathways Contributing to the Pathology.

作者信息

Licholai Sabina, Blaż Michal, Kapelak Boguslaw, Sanak Marek

机构信息

Division of Molecular Biology and Clinical Genetics, Department of Medicine, Jagiellonian University Medical College, Krakow, Poland.

Students' Research Group, Division of Molecular Biology and Clinical Genetics, Department of Medicine, Jagiellonian University Medical College, Krakow, Poland.

出版信息

Ann Thorac Surg. 2016 Oct;102(4):1245-52. doi: 10.1016/j.athoracsur.2016.03.061. Epub 2016 May 25.

Abstract

BACKGROUND

Complex etiopathogenesis of ascending aortic aneurysm suggests contribution of epigenetic mechanisms in its development. Several studies appointed microRNAs (miRs) as essential epigenetic factors in various human diseases; however, little is known about their role in ascending aortic aneurysm. Therefore, the aim of this study was to perform unbiased molecular screening of miRs expression in aneurysmal tissue and establish their functions on a transcriptional level.

METHODS

Samples of ascending aortic tissue were obtained from 15 patients, and total RNA was isolated separately from aneurysmal and unaffected aortic tissue obtained from the same patient. Expression of the complete panel of human miRs was assessed by quantitative real-time polymerase chain reaction. Using bioinformatic tools, 13 genes were selected that were putatively regulated by overexpressed miRs. Expression level of transcripts were evaluated by quantitative real-time polymerase chain reaction and correlated with their targeting miRs.

RESULTS

Overexpression of 10 miRs distinguished aneurysmal tissue from the unchanged one. These miRs were involved in cell senescence (miR-191-5p), maintenance of vascular integrity (miR-126-3p and miR-374-5p), nitric oxide-dependent vascular relaxation (miR-21-5p), smooth muscle differentiation, and contractility (miR-145- 3p, miR-29c-3p, miR-133a-3p, miR-186-5p, miR-143-3p, and miR-24-3p), and correlated with abundance of its miR targets.

CONCLUSIONS

Altered expression of particular miRs selectively in the affected tissue indicate their role as factors that trigger pathways of aneurysmal transformation. Limited reparative properties due to overexpression of miR-191 may play a crucial role for aneurysm enlargement, whereas nitric oxide-dependent relaxation of vascular smooth muscle mediated by miR-21 offers an attractive explanation of the aneurysm's initiation, and is confirmed in experimental conditions.

摘要

背景

升主动脉瘤复杂的发病机制提示表观遗传机制在其发展过程中发挥作用。多项研究表明,微小RNA(miR)是多种人类疾病中重要的表观遗传因子;然而,关于它们在升主动脉瘤中的作用却知之甚少。因此,本研究的目的是对动脉瘤组织中的miR表达进行无偏倚的分子筛选,并在转录水平上确定它们的功能。

方法

从15例患者获取升主动脉组织样本,分别从同一患者的动脉瘤组织和未受影响的主动脉组织中分离总RNA。通过定量实时聚合酶链反应评估人类miR完整面板的表达。使用生物信息学工具,选择了13个可能受过表达miR调控的基因。通过定量实时聚合酶链反应评估转录本的表达水平,并将其与其靶向miR相关联。

结果

10种miR的过表达可将动脉瘤组织与未改变的组织区分开来。这些miR参与细胞衰老(miR-191-5p)、血管完整性维持(miR-126-3p和miR-374-5p)、一氧化氮依赖性血管舒张(miR-21-5p)、平滑肌分化和收缩性(miR-145-3p、miR-29c-3p、miR-133a-3p、miR-186-5p、miR-143-3p和miR-24-3p),并与其miR靶标的丰度相关。

结论

特定miR在受影响组织中的表达改变表明它们作为触发动脉瘤转化途径的因子发挥作用。miR-191过表达导致的有限修复特性可能在动脉瘤扩大中起关键作用,而miR-21介导的一氧化氮依赖性血管平滑肌舒张为动脉瘤的起始提供了有吸引力的解释,并在实验条件下得到证实。

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